CFDAWatch offers synchronous updates of CFDA's regulations, notices and guidelines for the registration of pharmaceuticals and medical devices in China.



Pharmaceutical News

CFDA consults  on provisions for the joint evaluation of the registration of APIs, excipients and pharma packaging materials
CFDA consults on provisions for the joint evaluation of the registration of APIs, excipients and pharma packaging materials

2017-12-06
CFDA has published draft provisions for the joint evaluation of the registration of APIs, excipients and ...

CFDA publishes drug registration evaluation guides
CFDA publishes drug registration evaluation guides

2017-12-01
 CFDA publishes drug registration evaluation guides for the following types of pharmaceutical regist...

CFDA to adjust registration evaluation and approval of pharma packaging materials and excipients
CFDA to adjust registration evaluation and approval of pharma packaging materials and excipients

2017-12-01
CFDA has published a notice on its website to officially annouce that it revokes separate registration ev...

CDE consults on clinical trial technical guideline for acute heart failure
CDE consults on clinical trial technical guideline for acute heart failure

2017-11-29
CDE has published clinical trial technical guideline for acute heart failure (AHF) for public consultatio...

CDE to accept drug registration applications directly
CDE to accept drug registration applications directly

2017-11-29
The Center for Drug Evaluation (CDE) of CFDA has a notice on its website requesting drug registration app...

Medical Device News

CFDA issues provisions for the supervision and administration of online sales of medical devices
CFDA issues provisions for the supervision and administration of online sales of medical devices

2017-12-26
CFDA issues provisions for the supervision and administration of online sales of medical devices. The mea...

CFDA publishes provisions for the record-keeping and conditions for clinical trial organizations for medical devices
CFDA publishes provisions for the record-keeping and conditions for clinical trial organizations for medical devices

2017-11-24
CFDA and National Health and Familly Planning Commission (NHFPC) have jointly issued provisions for the r...

CFDA publishes guidelines for determining the registration units of medical device
CFDA publishes guidelines for determining the registration units of medical device

2017-11-24
CFDA publishes guidelines for determining the registration units of medical devices. The guidelines help ...

CFDA publishes new provisions for the supervision and administration of medical device operation(2017)
CFDA publishes new provisions for the supervision and administration of medical device operation(2017)

2017-11-22
 On 21 Nov 2017, CFDA publishes revised provisions for the supervision and administration of medical...

CFDA publishes revised provisions for the supervision and administration of medical device production(2017)
CFDA publishes revised provisions for the supervision and administration of medical device production(2017)

2017-11-22
 On 21 Nov 2017, CFDA publishes revised provisions for the supervision and administration of the pro...